RBM14-RBM4 RBM14-RBM4 readthrough

Information
Symbol
RBM14-RBM4
Type
protein-coding
Description
RBM14-RBM4 readthrough
Entrez Gene ID
100526737
Genome
hg19
Position
chr11:66,384,097-66,413,940
Genome
hg38
Position
chr11:66,616,626-66,646,469
HGNC
HGNC:38840 HGNC
Ensembl
ENSG00000248643 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
52
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM COAZ
SYNONYM PSP2
SYNONYM RBM14
SYNONYM SIP
HGNC HGNC:38840 HGNC
Ensembl ENSG00000248643 Ensembl
AllianceGenome HGNC:38840
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000500635.2 hg38 chr11 66,616,670 66,646,467 29,798
ENST00000412278.2 hg38 chr11 66,616,626 66,646,469 29,844
ENST00000412278.2 hg19 chr11 66,384,097 66,413,940 29,844
ENST00000500635.2 hg19 chr11 66,384,141 66,413,938 29,798
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